Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001720180 | SCV000523709 | likely benign | not provided | 2019-03-13 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002230038 | SCV001005164 | likely benign | Autosomal dominant epilepsy with auditory features | 2024-01-07 | criteria provided, single submitter | clinical testing |